510(k) K934401 ยท HRX Arthroscope
ARTHROTEK CANNULA SYSTEM
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Mar 24, 1994 |
| Received | Sep 9, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934401
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.